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Showing results (241-250 of 282) with videos related to

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European Journal of Human Genetics : EJHG|July 16, 2015
Missense variants in AIMP1 gene are implicated in autosomal recessive intellectual disability without neurodegenerationZafar Iqbal, Lucia Püttmann, Luciana Musante, et al.
Human Molecular Genetics|June 13, 2018
Biallelic missense variants in ZBTB11 can cause intellectual disability in humansZohreh Fattahi, Taimoor I Sheikh, Luciana Musante, et al.
American Journal of Medical Genetics. Part A|November 26, 2009
Genome-wide linkage scan of nonsyndromic orofacial clefting in 91 families of central European originElisabeth Mangold, Heiko Reutter, Stefanie Birnbaum, et al.
Theranostics|September 23, 2024
Theranostics with somatostatin receptor antagonists in SCLC: Correlation of <sup>68</sup>Ga-SSO120 PET with immunohistochemistry and survivalIlektra Antonia Mavroeidi, Anna Romanowicz, Tristan Haake, et al.
Addiction Biology|November 3, 2010
An integrated genome research network for studying the genetics of alcohol addictionRainer Spanagel, Dusan Bartsch, Bendikt Brors, et al.
Annals of Clinical and Translational Neurology|January 10, 2015
Mutations in PTRH2 cause novel infantile-onset multisystem disease with intellectual disability, microcephaly, progressive ataxia, and muscle weaknessHao Hu, Michelle L Matter, Lina Issa-Jahns, et al.
American Journal of Medical Genetics|September 5, 2002
No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1Thomas Sander, Christine Windemuth, Herbert Schulz, et al.
European Journal of Oral Sciences|February 4, 2010
IRF6 gene variants in Central European patients with non-syndromic cleft lip with or without cleft palateStefanie Birnbaum, Kerstin U Ludwig, Heiko Reutter, et al.
Molecular Psychiatry|April 28, 2001
A possible susceptibility locus for bipolar affective disorder in chromosomal region 10q25--q26S Cichon, G Schmidt-Wolf, J Schumacher, et al.
American Journal of Human Genetics|February 24, 2015
Homozygous SLC6A17 mutations cause autosomal-recessive intellectual disability with progressive tremor, speech impairment, and behavioral problemsZafar Iqbal, Marjolein H Willemsen, Marie-Amélie Papon, et al.
Pageof 29

Showing results (241-250 of 282) with videos related to

Sort By:
Pageof 29
European Journal of Human Genetics : EJHG|July 16, 2015
Missense variants in AIMP1 gene are implicated in autosomal recessive intellectual disability without neurodegenerationZafar Iqbal, Lucia Püttmann, Luciana Musante, et al.
Human Molecular Genetics|June 13, 2018
Biallelic missense variants in ZBTB11 can cause intellectual disability in humansZohreh Fattahi, Taimoor I Sheikh, Luciana Musante, et al.
American Journal of Medical Genetics. Part A|November 26, 2009
Genome-wide linkage scan of nonsyndromic orofacial clefting in 91 families of central European originElisabeth Mangold, Heiko Reutter, Stefanie Birnbaum, et al.
Theranostics|September 23, 2024
Theranostics with somatostatin receptor antagonists in SCLC: Correlation of <sup>68</sup>Ga-SSO120 PET with immunohistochemistry and survivalIlektra Antonia Mavroeidi, Anna Romanowicz, Tristan Haake, et al.
Addiction Biology|November 3, 2010
An integrated genome research network for studying the genetics of alcohol addictionRainer Spanagel, Dusan Bartsch, Bendikt Brors, et al.
Annals of Clinical and Translational Neurology|January 10, 2015
Mutations in PTRH2 cause novel infantile-onset multisystem disease with intellectual disability, microcephaly, progressive ataxia, and muscle weaknessHao Hu, Michelle L Matter, Lina Issa-Jahns, et al.
American Journal of Medical Genetics|September 5, 2002
No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1Thomas Sander, Christine Windemuth, Herbert Schulz, et al.
European Journal of Oral Sciences|February 4, 2010
IRF6 gene variants in Central European patients with non-syndromic cleft lip with or without cleft palateStefanie Birnbaum, Kerstin U Ludwig, Heiko Reutter, et al.
Molecular Psychiatry|April 28, 2001
A possible susceptibility locus for bipolar affective disorder in chromosomal region 10q25--q26S Cichon, G Schmidt-Wolf, J Schumacher, et al.
American Journal of Human Genetics|February 24, 2015
Homozygous SLC6A17 mutations cause autosomal-recessive intellectual disability with progressive tremor, speech impairment, and behavioral problemsZafar Iqbal, Marjolein H Willemsen, Marie-Amélie Papon, et al.
Pageof 29